🏥 Medical Devices Class I - Dangerous
Zimmer Biomet Inc. initiated a field action on 02/28/2017 for sterile-packaged implants packaged in two different package configurations due to packaging design verification test failures.
All Recalls
95,083 total recalls in our database
Fem IM Nail 15mmdx44cm, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants
Zimmer Biomet
🏥 Medical Devices Class I - Dangerous
Zimmer Biomet Inc. initiated a field action on 02/28/2017 for sterile-packaged implants packaged in two different package configurations due to packaging design verification test failures.
GE Healthcare Discovery NM/CT 670 CZT X-ray system
GE Healthcare
🏥 Medical Devices Class I - Dangerous
It was discovered that an issue has been identified that can result in a scan starting before the prescribed delay has completed.
🏥 Medical Devices Class I - Dangerous
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
🏥 Medical Devices Class I - Dangerous
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
🏥 Medical Devices Class I - Dangerous
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
🏥 Medical Devices Class I - Dangerous
Cook Inc. is initiating a voluntary recall of the Vue Optic Visualization Source and the Flexor Vue Deflecting Endoscopic System because it was determined that the current reprocessing instructions do not provide sufficient detailed information for the cleaning, disinfection, and sterilization of these products.
🏥 Medical Devices Class I - Dangerous
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
🏥 Medical Devices Class I - Dangerous
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
🏥 Medical Devices Class I - Dangerous
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
🏥 Medical Devices Class I - Dangerous
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
GE Healthcare Optima CT660, CT680 X-ray system
GE Healthcare
🏥 Medical Devices Class I - Dangerous
It was discovered that an issue has been identified that can result in a scan starting before the prescribed delay has completed.
🏥 Medical Devices Class I - Dangerous
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
🏥 Medical Devices Class I - Dangerous
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
🏥 Medical Devices Class I - Dangerous
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
Por fullct fem st 20x200mm, Sterile, Rod, fixation, intramedullary and accessories- Specific Knee, Hip and Nail Implants
Zimmer Biomet
🏥 Medical Devices Class I - Dangerous
Zimmer Biomet Inc. initiated a field action on 02/28/2017 for sterile-packaged implants packaged in two different package configurations due to packaging design verification test failures.
🏥 Medical Devices Class I - Dangerous
One lot of CADD¿ High Volume Administration sets, part number 21-7381-24, lot number 26X035, incorrectly contained the IFU insert for part number 21-7357-24.
4.5 BROAD SCP PLT 26-H STER
Zimmer Biomet
🏥 Medical Devices Class I - Dangerous
Zimmer Biomet is initiating a field action for sterile-packaged implants packaged in a single package configuration due to packaging design verification test failures.
VITEK¿ 2 Gram Negative Susceptibility card (AST-N208), IVD, REF 413062, 20 cards per carton.
Biomerieux
🏥 Medical Devices Class I - Dangerous
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).
🏥 Medical Devices Class I - Dangerous
The integrity of the product container may be compromised thereby exposing product to moisture which could lead to antibiotic degradation (loss of potency).